516 results
Allele/Variant Genes: H2-K1 (Mmu)

H2-K1em2Smoc

(Mus musculus)
Allele/Variant
Source: MGI:6446870
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1b-em5Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7290150
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1b-em6Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7290151
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:6452604
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1b-em1Tyj

(Mus musculus)
Allele/Variant
Source: MGI:7382781
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1b-em3Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7264553
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1b-tm1Bpe

(Mus musculus)
Allele/Variant
Source: MGI:1931444
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1d-em2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7377556
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1d-em5Dvs

(Mus musculus)
Allele/Variant
Source: MGI:6118979
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1d-em1Dvs

(Mus musculus)
Allele/Variant
Source: MGI:6119459
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:7290149
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1b-em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:6446897
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7766166
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1d-em6Dvs

(Mus musculus)
Allele/Variant
Source: MGI:6118986
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1d-em4Dvs

(Mus musculus)
Allele/Variant
Source: MGI:6118907
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1b-em1Erob

(Mus musculus)
Allele/Variant
Source: MGI:7628344
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1b-em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7300073
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

H2-K1d-em7Dvs

(Mus musculus)
Allele/Variant
Source: MGI:6118982
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs387487973
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34219320G>A

Allele/Variant
Source: rs214064625
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215136T>C

Allele/Variant
Source: rs108517543
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215177C>A

Allele/Variant
Source: rs581500900
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34216504C>G

Allele/Variant
Source: rs578942079
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34216531G>A

Allele/Variant
Source: rs217412222
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217866T>A

Allele/Variant
Source: rs108558196
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217705G>C

Allele/Variant
Source: rs1132256169
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217714A>G

Allele/Variant
Source: rs220537569
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34218132C>G

Allele/Variant
Source: rs1134022860
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34218547T>C

Allele/Variant
Source: rs1133300139
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34216957C>A

Allele/Variant
Source: rs583713792
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34216968G>A

Allele/Variant
Source: rs1134232325
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217064C>T

Allele/Variant
Source: rs387614746
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217270T>C

Allele/Variant
Source: rs48654368
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34216612G>T

Allele/Variant
Source: rs255973596
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217661G>A

Allele/Variant
Source: rs107920699
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217673C>T

Allele/Variant
Source: rs258990172
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34218135C>T

Allele/Variant
Source: rs578583948
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34218262G>T

Allele/Variant
Source: rs587164179
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34218738G>C

Allele/Variant
Source: rs582514397
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34216224C>T

Allele/Variant
Source: rs1132988437
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215946C>T

Allele/Variant
Source: rs215838515
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215174T>C

Allele/Variant
Source: rs108185637
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215450G>A

Allele/Variant
Source: rs107809864
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34216496C>G

Allele/Variant
Source: rs1133453794
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217702A>T

Allele/Variant
Source: rs108483887
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34217825T>A

Allele/Variant
Source: rs584704826
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34218446A>C

Allele/Variant
Source: rs251302715
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34218396C>G

Allele/Variant
Source: rs1133580638
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34218495A>G

Allele/Variant
Source: rs1133365110
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34215610A>T

Allele/Variant
Source: rs1133966869
Genes: H2-K1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:34216661G>T